Clinical Trial Manager, Oncology Experience Required

🔥 23 minutes ago

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

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Parexel

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1983

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 Venture Round on 1990-01

Consulting • Healthcare • Logistics

Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.

📋 Description

• Deliver committed country-level components of clinical studies within agreed timelines, budgets, and resource plans • Ensure compliance with client procedures, ICH-GCP guidelines, and local regulations • Lead and optimize Local Study Team performance at country level • Manage country-level study budgets and maintain accurate financial information through regular review of study financial systems and reports • Prepare country financial Study Management Agreements (fSMA) in a timely manner • Oversee preparation of country-level Master Informed Consent Forms, site-specific informed consent documentation, and required translations • Ensure timely submission of applications and study-related documentation to Ethics Committees and Institutional Review Boards throughout the study lifecycle • Collaborate with internal and external stakeholders for efficient study delivery and effective cross-functional partnership • Support study quality and operational excellence while maintaining regulatory and client-standard compliance • Lead local study delivery for a single client and contribute to country-level clinical trial programs

🎯 Requirements

• Bachelor's degree or equivalent experience in a relevant scientific, healthcare, or clinical research discipline • Minimum of 3 years' experience running local clinical trials • Experience in oncology clinical trials • Proven ability to lead and motivate cross functional teams to deliver clinical trials on time, within budget, and to required quality standards • Good understanding and working knowledge of clinical research, clinical trial phases, ICH-GCP, and applicable country clinical research regulations and guidelines • Experience performing submissions to Regulatory Authorities (RA) and Ethics Committees (EC) • Strong leadership, team motivation, and stakeholder management capabilities • Experience working within clinical research and local clinical trial delivery environments • Ability to collaborate effectively across cross functional teams • Excellent organizational, time management, and problem-solving skills, with ability to manage multiple priorities • Quality-focused approach and commitment to regulatory compliance and study excellence • Confidence working with study financial systems, regulatory processes, and clinical trial documentation • Preferred: Monitoring experience within oncology clinical studies • Preferred: Experience partnering with study functions to support smooth and effective study delivery

🏖️ Benefits

• Medical & Dental Insurance • Life Assurance • Pension • Critical Illness Insurance & Health Screenings • Comprehensive benefits package for eligible employees, including life assurance, medical and dental insurance, and additional benefit offerings in accordance with applicable plans • Flexibility • Professional development and career growth opportunities

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